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Biotin-PEG(3)-NH2
Nom chimique: N-[2-[2-[2-(2-Aminoethoxy)ethoxy]ethoxy]ethyl]biotinamide // Synonymes: Biotin-PEG3-Amine, N-Biotinyl-3,6,9-trioxaundecane-1,11-diamine, Amine-PEG3-Biotin, Biotinyl-PEG3-NH2,N-(2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)ethyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]im idazol-4-yl)pentanamide
- n° Art.:RL-4210
- n° CAS:359860-27-8
- Formule:C18H34N4O5S
- Storage temperature:-20°C
- Masse moléculaire:418,22 g/mol
- Pureté:min.97%
from 100,00 €
description
Biotinylation reagent.
references
Serum apolipoprotein A-I potentiates the therapeutic efficacy of lysocin E against Staphylococcus aureus; H. Hamamoto, S. Panthee, A. Paudel, K. Ishii, J. Yasukawa, J. Su, A. Miyashita, H. Itoh, K. Tokumoto, M. Inoue, K. Sekimizu; Nat Commun 2021, 12: 6364. https://doi.org/10.1038/s41467-021-26702-0
Chiral Quantum Metamaterial for Hypersensitive Biomolecule Detection; M. Hajji, M. Cariello, C. Gilroy, M. Kartau, C. D. Syme, A. Karimullah, N. Gadegaard, A. Malfait, P. Woisel, G. Cooke, W. J. Peveler, M. Kadodwala; ACS Nano 2021; 15(12): 19905-19916. https://doi.org/10.1021/acsnano.1c07408
Dissecting the molecular determinants of clinical PARP1 inhibitor selectivity for tankyrase1; K. Ryan, B. Bolaòos, M. Smith, P. B. Palde, P. D. Cuenca, T. L. VanArsdale, S. Niessen, L. Zhang, D. Behenna, M. A. Ornelas, K. T. Tran, S. Kaiser, L. Lum, A. Stewart, K. S. Gajiwala; J. Biol. Chem. 2021; 296: 100251. https://doi.org/10.1074/jbc.RA120.016573
Biotinylated Phosphorus Dendrimers as Control Line in Nucleic Acid Lateral Flow Tests; L. Vidal, A. B. Aissa, J. Salabert, J. J. Jara, A. Vallribera, M. I. Pividori, R. M. Sebastián; Biomacromolecules 2020; 21 (3): 1315–1323. https://doi.org/10.1021/acs.biomac.0c00161
Bioorthogonal Ligation and Cleavage by Reactions of Chloroquinoxalines with ortho-Dithiophenols; Y. Li, Z. Lou, H. Li, H. Yang, Y. Zhao, H. Fu; Angew. Chem. Int. Ed. 2020; 59(9): 3671-367. https://doi.org/10.1002/anie.201913620
COMBINES-CID: An Efficient Method for De Novo Engineering of Highly Specific Chemically Induced Protein Dimerization Systems; S. Kang, K. Davidsen, L. Gomez-Castillo, H. Jiang, X. Fu, Z. Li, Y. Liang, M. Jahn, M. Moussa, F. DiMaio, L. Gu; J. Am. Chem. Soc. 2019, 141(28): 10948–10952. https://doi.org/10.1021/jacs.9b03522
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All information contained in our webshop is compiled to the best of our knowledge.
Prices and product availability are subject to change and require reconfirmation. Please contact us for further information.
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